NDC 69491-101 Delta Sky Club
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69491 - Buzz Export Services Pty Ltd
- 69491-101 - Delta Sky Club
Product Packages
NDC Code 69491-101-00
Package Description: 1 KIT in 1 KIT * 1 TUBE in 1 CARTON (69491-060-94) / 10 g in 1 TUBE
Product Details
What is NDC 69491-101?
What are the uses for Delta Sky Club?
Which are Delta Sky Club UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Delta Sky Club Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
What is the NDC to RxNorm Crosswalk for Delta Sky Club?
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.0076 MG/MG Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )Toothpaste
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".